A new compound [mpba][Cu_2Br_3]（1, mpba = 4-（N-methylpyridin-4-yl）benzoic acid） has been ionothermally synthesized and characterized by single-crystal X-ray diffraction analysis, infrared spectrum, elemental analy...A new compound [mpba][Cu_2Br_3]（1, mpba = 4-（N-methylpyridin-4-yl）benzoic acid） has been ionothermally synthesized and characterized by single-crystal X-ray diffraction analysis, infrared spectrum, elemental analyses, fluorescence spectrum, and thermogravimetric analysis. In compound 1, the [mpba]＋ cation is a new organic template, which is obtained firstly in this work by in situ alkylation reaction of N-heterocycles 4-（pyridin-4-yl）benzoic acid with [Emim]Br（Emim = 1-ethyl-3-methyl imidazolium）. Hirshfeld surface analysis shows that weak interactions between the [mpba]＋ cations and 1D inorganic [Cu_2Br_3]~– are mainly C–H···Br hydrogen bonds. In addition, a pairwise O–H···O interaction is observed between the adjacent [mpba]＋cations. These different types of weak interactions make compound 1 stable up to 300 ℃. Fluorescence spectrum investigation shows 1 has a strong yellow emission at 555 nm. Theoretical calculation not only demonstrates compound 1 is a wild band semiconductor with a 3.3 e V band gap but also elucidates the fluorescence emission derives from the p-π＊ transition of electrons from [Cu_2Br_3]~– to [mpba]~＋.展开更多
The polymerization behaviors of Styrene (St) in the presence of CuX/L [X=Cl or Br; L= 2,2 bipyridine (bpy), 1,10 phenanthroline (phen) or 4,7 diphenyl 1,10 phenanthroline (DPP) ] and R X (R=trichloromethyl, benz...The polymerization behaviors of Styrene (St) in the presence of CuX/L [X=Cl or Br; L= 2,2 bipyridine (bpy), 1,10 phenanthroline (phen) or 4,7 diphenyl 1,10 phenanthroline (DPP) ] and R X (R=trichloromethyl, benzyl or allyl; X=Cl or Br) have been studied and examined. In a CuCl/bpy/RCl/St system, a bimodal GPC peak at the early stage of polymerization was observed, and a concept of multi active species was proposed to explain this phenomenon. In a CuCl/phen (DPP)/RCl/St system, the \%M\%\-n of polystyrene (PS) increased linearly with St conversion and ln[M] o/[M] also increased linearly with time, indicating the living nature of this system. Furthermore, the stability of the propagating active species in a CuBr/phen/RBr/St system is higher than that in the CuBr/phen/RBr/St system.展开更多
A CuX-mediated regioselective halogenation reaction of 2-phenylimidazo[1,2-a]pyridine in the presence of oxygen is introduced in this paper.This reaction provides an effective method for the production of C-3 halogena...A CuX-mediated regioselective halogenation reaction of 2-phenylimidazo[1,2-a]pyridine in the presence of oxygen is introduced in this paper.This reaction provides an effective method for the production of C-3 halogenated 2-phenylimidazo[1,2-a]pyridines with a yield of up to 96%.A plausible mechanism for the formation of title compounds via 2-phenylimidazo[1,2-a]pyridine–CuX complex intermediate is proposed.The structure of representative compounds is established by the single crystal XRD method.The electronic structure,corroborated by Hirshfeld surface analysis and DFT calculations,rationalizes characters of relevant absorptions and emission as well as large Stokes shifts.展开更多
基金supported by the Natural Science Foundation of Fujian Province(No.2014J01029)
文摘A new compound [mpba][Cu_2Br_3]（1, mpba = 4-（N-methylpyridin-4-yl）benzoic acid） has been ionothermally synthesized and characterized by single-crystal X-ray diffraction analysis, infrared spectrum, elemental analyses, fluorescence spectrum, and thermogravimetric analysis. In compound 1, the [mpba]＋ cation is a new organic template, which is obtained firstly in this work by in situ alkylation reaction of N-heterocycles 4-（pyridin-4-yl）benzoic acid with [Emim]Br（Emim = 1-ethyl-3-methyl imidazolium）. Hirshfeld surface analysis shows that weak interactions between the [mpba]＋ cations and 1D inorganic [Cu_2Br_3]~– are mainly C–H···Br hydrogen bonds. In addition, a pairwise O–H···O interaction is observed between the adjacent [mpba]＋cations. These different types of weak interactions make compound 1 stable up to 300 ℃. Fluorescence spectrum investigation shows 1 has a strong yellow emission at 555 nm. Theoretical calculation not only demonstrates compound 1 is a wild band semiconductor with a 3.3 e V band gap but also elucidates the fluorescence emission derives from the p-π＊ transition of electrons from [Cu_2Br_3]~– to [mpba]~＋.
文摘The polymerization behaviors of Styrene (St) in the presence of CuX/L [X=Cl or Br; L= 2,2 bipyridine (bpy), 1,10 phenanthroline (phen) or 4,7 diphenyl 1,10 phenanthroline (DPP) ] and R X (R=trichloromethyl, benzyl or allyl; X=Cl or Br) have been studied and examined. In a CuCl/bpy/RCl/St system, a bimodal GPC peak at the early stage of polymerization was observed, and a concept of multi active species was proposed to explain this phenomenon. In a CuCl/phen (DPP)/RCl/St system, the \%M\%\-n of polystyrene (PS) increased linearly with St conversion and ln[M] o/[M] also increased linearly with time, indicating the living nature of this system. Furthermore, the stability of the propagating active species in a CuBr/phen/RBr/St system is higher than that in the CuBr/phen/RBr/St system.
基金supported by the National Natural Science Foundation of China(22171105 and 12004384)Shandong Provincial Natural Science Foundation(ZR2020KB012,ZR2021MB001,and ZR2022YQ14)+1 种基金the Fund of State Key Laboratory of Structural Chemistry(20210015)the Special Foundation of Taishan Scholar Project.
基金the National Natural Science Foundation of China(No.21105091)for financial support.
文摘A CuX-mediated regioselective halogenation reaction of 2-phenylimidazo[1,2-a]pyridine in the presence of oxygen is introduced in this paper.This reaction provides an effective method for the production of C-3 halogenated 2-phenylimidazo[1,2-a]pyridines with a yield of up to 96%.A plausible mechanism for the formation of title compounds via 2-phenylimidazo[1,2-a]pyridine–CuX complex intermediate is proposed.The structure of representative compounds is established by the single crystal XRD method.The electronic structure,corroborated by Hirshfeld surface analysis and DFT calculations,rationalizes characters of relevant absorptions and emission as well as large Stokes shifts.
